THE COURSE OF ISCHEMIC HEART DISEASE IN A PATIENT WITH HEREDIC THROMBOPHILIA BASED ON A MUTATION IN THE PAI-1 GENE (CLINICAL CASE)
DOI:
https://doi.org/10.11603/1811-2471.2021.v.i2.12227Keywords:
coronary artery disease, plasminogen activator inhibitor 1, gene mutations, thrombosis, acute coronary syndromeAbstract
Genetically determined hemostasis defects can often increase the risk of thrombotic events.
The aim – to find out the features of coronary artery disease (CHD) in a patient with a mutation in the PAI-1 gene.
Material and Methods. The course of coronary artery disease was analyzed taking into account the history, the results of laboratory tests, ECG data, echocardiography, coronary angiography.
Results. The course of coronary artery disease was characterized by frequent hospitalizations for acute coronary syndrome and steady progression of atherosclerotic changes in the coronary arteries. Dual antithrombotic therapy (rivaroxaban, 15 mg; clopidogrel, 75 mg daily) and high-intensity statin therapy reduced coronary events.
Conclusions. Diagnosing of hereditary thrombophilia and optimization of treatment strategy can improve the course of coronary artery disease.
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